(Q80524662)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

title

Spinal muscle atrophy type 1 (Werdnig-Hoffman disease) with complex cardiac malformation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

main subject

Werdnig–Hoffmann disease

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

author name string

Sunanda Kotagiri

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Duncan Cameron

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

Ian Peart

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

publication date

1 June 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

1 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

volume

163

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

page(s)

331-332

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15346918%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00431-004-1437-6

1 January 2020

exact match

0 references

cites work

Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: a lethal condition

1 reference

12 December 2020

Spinal muscular atrophy type I combined with atrial septal defect in three sibs.

1 reference

12 December 2020

Clinical and molecular genetic features of congenital spinal muscular atrophy.

1 reference

12 December 2020

Cardiac involvement in Werdnig-Hoffmann's spinal muscular atrophy

1 reference

12 December 2020

Spinal muscular atrophy combined with congenital heart disease: a report of two cases.

1 reference

12 December 2020

SMN gene deletion in variant of infantile spinal muscular atrophy

1 reference

12 December 2020

Spinal muscular atrophy: recent advances and future prospects.

1 reference

12 December 2020